Label: ALCOHOL PREP PAD- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 1, 2010

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  • ACTIVE INGREDIENT

    Isopropyl Alcohol 70% v/v

  • PURPOSE

    Antiseptic

  • USE

    For preparation of the skin prior to an injection
  • WARNINGS

    For external use only.
    Flammable, keep away from fire or flame.

    Do not use

    • with electrocautery procedures
    • in the eyes

    Stop use

    if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.






    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    Wipe injection site vigorously and discard.
  • SPL UNCLASSIFIED SECTION


  • OTHER INFORMATION

    Store at room temperature 15°- 30° C (59° - 86° F)
  • INACTIVE INGREDIENT

    purified water
  • Questions?

    Call 1-800-910-6874

  • PACKAGE INFORMATION

    up and up

    NDC 11673-600-10

    alcohol prep pads
    70% isopropyl alcohol

    Compare to BD®*

    antiseptic for preparation of skin prior to injection

    100 count

    100 INDIVIDUALLY WRAPPED PADS

    Distributed by Target Corporation
    Minneapolis, MN 55403
    Made in U.S.A.

    © 2009 Target Brands, Inc.
    All Rights Reserved
    Shop Target.com

    *This product is not manufactured or distributed by Becton Dickinson and Company, owner of the registered trademark BD®.

    image of carton
  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl alcohol (UNII: ND2M416302) (Isopropyl alcohol - UNII:ND2M416302) Isopropyl alcohol0.70 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-600-10100 in 1 BOX
    11 in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/01/2008
    Labeler - Target Corporation (006961700)
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